Lifecore Biomedical offer service "Contract Development and Manufacturing"
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Service Name
Contract Development and Manufacturing
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Specifications
- Regulatory Certification: Operates as an FDA-approved CDMO ensuring the final process is scalable and successfully transfers to a cGMP-compliant commercial manufacturing process.
- Batch Size Range: Decades of experience producing highly viscous sodium hyaluronate formulations, supporting the full parenteral drug development programme from early process work to commercial scale.
- Packaging Format: Offers expertise in sterile filtration and aseptic filling for unique products that are challenging to formulate, applicable across the parenteral packaging format range.
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